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	Enantioselective synthesis of β-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative
	HE Ming; PAN ZhaoXi; BAI Song; LI Pei; ZHANG YuPing; JIN LinHong; HU DeYu; YANG Song; SONG BaoAn
	2013
期号	3页码:321-328
关键词	生物催化反应 金鸡纳生物碱 对映选择性合成 喹唑啉 氨基 Mannich反应 二羰基化合物 酯
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6473682
专题	贵州大学
作者单位	1.[1]State Key Laboratory Breeding Base of Green Pesticides and Agricultural Bioengineering 2.[2]Key Laboratory of Green Pesticides and Agricultural Bioengineering,Ministry of Education 3.[3]Guizhou University
推荐引用方式 GB/T 7714	HE Ming,PAN ZhaoXi,BAI Song,et al. Enantioselective synthesis of β-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative[J],2013(3):321-328.
APA	HE Ming.,PAN ZhaoXi.,BAI Song.,LI Pei.,ZHANG YuPing.,...&SONG BaoAn.(2013).Enantioselective synthesis of β-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative.(3),321-328.
MLA	HE Ming,et al."Enantioselective synthesis of β-amino esters bearing a quinazoline moiety via a Mannich-type reaction catalyzed by a cinchona alkaloid derivative"..3(2013):321-328.

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